Neuropsychiatric Disease and Treatment 2016:12 1333–1339
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investigating analgesic and psychological factors
associated with risk of postpartum depression
development: a case–control study
Thangavelautham suhitharan1
Thi Phuong Tu Pham2
helen chen2,3
Pryseley Nkouibert assam4
rehena sultana2
Nian-lin reena han5
ene-choo Tan6,7
Ban leong sng1,2
1Department of Women’s anaesthesia,
KK Women’s and children’s hospital,
2Duke-NUs Medical school, 3Women’s
service, Department of Psychological Medicine, KK Women’s and children’s hospital, 4singapore clinical research
institute, 5Division of clinical support
services, 6research laboratory, KK
Women’s and children’s hospital,
7singhealth Paediatrics academic
clinical Programme, Duke-NUs Medical school, singapore
Aim: The aim of this study was to investigate the role of peripartum analgesic and psychological factors that may be related to postpartum depression (PPD).
Methods: This case–control study was conducted in pregnant females who delivered at KK Women’s and Children’s Hospital from November 2010 to October 2013 and had postpartum psychological assessment. Demographic, medical, and postpartum psychological status assess-ments, intrapartum data including method of induction of labor, mode of labor analgesia, duration of first and second stages of labor, mode of delivery, and pain intensity on hospital admission and after delivery were collected. PPD was assessed using the Edinburgh Postnatal Depression Scale and clinical assessment by the psychiatrist.
Results: There were 62 cases of PPD and 417 controls after childbirth within 4–8 weeks. The odds of PPD was significantly lower (33 of 329 [10.0%]) in females who received epidural analgesia for labor compared with those who chose nonepidural analgesia (29 of 150 [19.3%]) ([odds ratio] 0.47 (0.27–0.8), P=0.0078). The multivariate analysis showed that absence of labor epidural analgesia, increasing age, family history of depression, history of depression, and previous history of PPD were independent risk factors for development of PPD.
Conclusion: The absence of labor epidural analgesia remained as an independent risk factor for development of PPD when adjusted for psychiatric predictors of PPD such as history of depression or PPD and family history of depression.
Keywords: epidural analgesia, childbirth, Edinburgh Postnatal Depression Scale
Introduction
Pregnancy and childbirth are significant events in a woman’s life. Childbirth is associated with complex physiological, psychological, and social interaction. Extreme labor pain, complicated prolonged labor, and a sense of lack of control are known to traumatize the childbirth experience and lead to postpartum depression (PPD), which affects the health of mothers and their newborns and is associated with long-term psychological and socioeconomic impact.1,2
PPD is defined in the Diagnostic and Statistical Manual for Mental Disorders as major depression with postpartum onset with episodes of depression beginning within 4 weeks of giving birth.3 PPD is significant as it may last up to 6 months after
delivery with significant public health impact on maternal health and child develop-ment.4 The incidence of PPD varies between studies depending on the time of survey
postdelivery and population being investigated. PPD occurs in ~10%–20% of females in the US5 and ~8% of females in Singapore.6 A recent study assessing depressive
symptoms using Edinburgh Postnatal Depression Scale (EPDS) in parturients at
correspondence: Ban leong sng Department of Women’s anaesthesia, KK Women’s and children’s hospital, 100 Bukit Timah road, singapore 229899, singapore
Tel +65 6394 1081 Fax +65 6291 2661
email sng.ban.leong@singhealth.com.sg
Journal name: Neuropsychiatric Disease and Treatment Article Designation: Original Research
Year: 2016 Volume: 12
Running head verso: Suhitharan et al
Running head recto: Mode of analgesia and risk of postpartum depression DOI: http://dx.doi.org/10.2147/NDT.S105918
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suhitharan et al
third trimester of pregnancy and 3 months postpartum by Verreault et al7 reported a higher rate of depressed mood
up to 16.4% at 3 months postpartum. Another prospective cohort study in parturients admitted for a vaginal delivery by Ding et al8 reported the incidence of PPD was 24.3% at 6
weeks postpartum, when PPD was defined by a score of 10 or more on EPDS. Contributing factors for development of PPD are multifactorial, including psychological, physical, social, and obstetric factors.9,10 These factors include pain
vulnerability and severity pain during childbirth, analgesic technique used during labor, and psychological and genetic susceptibility of the woman.9,11
Pain during childbirth has been described as one of the worst pain females may experience in her life.12 A
longitudi-nal cohort study alongitudi-nalyzing 1,288 deliveries in the US tertiary care center reported that one of five females after cesarean delivery and one of 13 females after vaginal delivery suffer from severe acute pain.13 The same study also identified
severity of acute postpartum pain as an independent risk factor for development of persistent pain and depression. Previous studies have identified a strong link between the intensity of labor pain with posttraumatic stress and mood disorders in the early postpartum period. Soet et al14 described
pain during labor was correlated with the development of posttraumatic stress disorder. Studies evaluating the severity of labor pain in the early postpartum period also found the correlation with postpartum blues15 and PPD.11 An earlier
study by Hiltunen et al16 found that females who received
epidural or paracervical block during their labor had lower depressive scores in the initial week after delivery compared with having no analgesia at all (odds ratio [OR] 0.25, 95% confidence interval [CI] 0.09–0.72). However, paracervical block is rarely performed limiting its applicability to daily routine practice. On the other hand, these early results are consistent with the idea that more complete pain control (using epidural analgesia) may reduce PPD.
With modern obstetric practice, females have several pain relief options during childbirth. However, the implications of analgesic choice may have greater effect than pain relief itself. Epidural analgesia is considered to be the gold standard of pain relief during labor. This procedure effectively blocks the pain transmission through the spinal cord and yet allows mothers to participate fully in the laboring process with no sedation. In a recent prospective cohort study, Ding et al8 reported that
epidu-ral analgesia is associated with lower occurrence of PPD com-pared with those who did not receive any labor analgesia.
Parturients undergoing childbirth have several anal-gesic choices including epidural, opioid, and Entonox analgesia in current practice. As Ding et al8 compared
epidural analgesia with no analgesia only, there is still a gap in knowledge with regard to other analgesic choices on the risk of PPD. Diagnosing PPD with EPDS, which is a screening tool, is also another controversial point that may overestimate the true incidence of PPD. Our study aims to investigate the role of potential peripartum analgesic and psychological factors that may be related to clinically confirmed PPD.
Methods
This study protocol was developed according to the Strengthening the Reporting of Observational studies in Epidemiology guidelines for reporting case–control stud-ies and was reviewed and approved by the SingHealth Centralized Institutional Review Board. SingHealth Central-ized Institutional Review Board registration: 2010/539/F. ClinicalTrials.gov registration: NCT02373709. Written informed consent was obtained from all the participants during the postpartum screening with EPDS.
This case–control study was conducted at KK Women’s and Children’s Hospital, Singapore from November 2010 to October 2013 in females who had their delivery and subse-quently participated in the postpartum psychological assess-ment program. The exclusion criteria included adolescent mothers (age ,18 years), females with stillbirth, or early neonatal loss. Medical records including epidural charts, partum monitoring charts, and the psychology notes at post-partum screening and consultation were reviewed. Information regarding peripartum events including peripartum obstetric data and PPD status was obtained for the data analysis.
We sought the following data from the available medical records: baseline data including age, weight, height, body mass index, and race. Socioeconomic status such as occu-pation, education level, type of housing, marital status, and number of children were self-reported. Obstetric history including parity, gestational age, and history of obstetric complications in current pregnancy including premature rupture of membrane were collected.
Intrapartum data including method of induction of labor, mode of labor analgesia, duration of first and second stages of labor, mode of delivery, and numeric rating scale pain score (11-point scale: 0 being no pain and 10 being the worst pain imaginable) on admission to labor ward and after delivery, occurrence of maternal pyrexia were documented.
The patients who came for routine postnatal consultations at the obstetrics clinics were screened and recruited via the postnatal screening program conducted by the Department of Psychological Medicine. Controls were obstetric patients who scored ,7 on the EPDS. Cases were defined as patients
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with confirmed clinical diagnosis of PPD as assessed at the outpatient clinic by board-certified psychiatrists using the
Diagnostic and Statistical Manual for Mental Disorders
criteria for major depression of postpartum onset.17 These
patients were referred from screening in the clinic or from the obstetric wards. Patients with psychotic disorders, comorbid predominant anxiety, or substance abuse were excluded. We used the Chinese version of EPDS validated in Singaporean peripartum females, if females could only speak Chinese.18
Data were summarized by cases (PPD) and controls (non-PPD) using mean (standard deviation) or median (range) for continuous variables as appropriate and number (pro-portions) of patients for categorical variables. OR together with corresponding 95% CI were used to characterize the association between PPD development and demographic, maternal medical history, perinatal, analgesic, and psycho-logical factors. Unadjusted and adjusted ORs were estimated using univariate and multivariate logistic regression analysis, respectively. The multivariate analysis was performed based on factors identified by univariate analyses with
P#0.2. Significance level was set at 5%, and all tests were
two-sided. SAS Version 9.3 software (SAS Institute Inc., Cary, NC, USA) was used for the analyses.
Results
Our data with a total of 744 patients who have delivered during the November 2010 to October 2013 and attended postpartum psychological assessment were reviewed in the study. Two hundred and fifty-four patients were excluded due to lack of labor analgesic data and eleven due to lack of confirmed PPD status. Data obtained from 479 patients were used for the analysis. There were 62 cases of PPD and 417 controls (without PPD) assessed within 4–8 weeks after childbirth.
The mean age (standard deviation) of the patients was 31.2 (4.9) years (range 19–48) (Table 1). Four hundred and seventy-two of 479 females (98.5%) were Chinese. Almost all females were married; only one woman was single. Seventy-five percent of females had a university education, 23.8% had middle education such as secondary school or junior college, and 1.5% had basic education of primary school level. Sixty-three percent of these females
Table 1 Demographic characteristics (n=479)
Characteristics Case (n=62) Control (n=417) Unadjusted OR (95% CI) P-value
age (years), mean (sD) 33.76 (6.25) 30.84 (4.6) 2.92 (1.62–4.21) ,0.0001
chinese, n (%)
No 2 (3.23) 5 (1.2) reference
Yes 60 (96.77) 412 (98.8) 0.36 (0.07–1.92) 0.2260
highest education level, n (%) 0.0875c
Primary or below 3 (4.84) 4 (0.96) 5.49 (1.19–25.39) 0.0385
secondary/junior college 16 (25.81) 98 (23.5) 1.20 (0.65–2.22) 0.1562
Postgraduate 43 (69.35) 315 (75.54) reference
Occupation, n (%) 0.4572
homemaker/unemployed 23 (37.1) 123 (29.5) reference 0.2174
Management 23 (37.1) 165 (39.57) 0.75 (0.40–1.39) 0.7541
Others 16 (25.81) 129 (30.94) 0.66 (0.34–1.32) 0.3936
Marital status, n (%)a 0.1294b
Married 61 (98.39) 417 (100)
single 1 (1.61) 0 (0.0)
Number of children, mean (sD) 1.73 (0.89) 1.48 (0.72) 1.46 (1.07–2.00) 0.0188
Weight (kg) – current, mean (sD) 59.83 (11.07) 59.12 (8.99) 1.01 (0.98–1.04) 0.5762
Weight (kg) – before pregnancy, mean (sD) 55.83 (10.55) 54.22 (9.58) 1.02 (0.99–1.04) 0.2317
BMi – current, mean (sD) 23.39 (3.98) 30.02 (49.13) 0.99 (0.97–1.02) 0.4581
BMi – before pregnancy, mean (sD) 27.9 (47.29) 22.15 (19.87) 1.01 (1.00–1.01) 0.1536
Pregnancy, n (%)
Planned-assisted 36 (58.06) 266 (63.79) 0.79 (0.46–1.35) 0.3843
Unplanned 26 (41.94) 151 (36.21) reference
expected childcare, n (%)
childcare/nursery 30 (48.39) 258 (61.87) 0.58 (0.34–0.99) 0.0448
self/partner 32 (51.61) 159 (38.13) reference
Notes: Case represents patients with clinically confirmed diagnosis of PPD using DSM IV criteria of major depression of postpartum onset. control represents non-PPD patients with ePDs score #7. Unadjusted Ors were obtained from univariate logistic regression. aOr cannot be estimated for marital status due to zero count. bP-value was
calculated based on Fisher’s exact test. cType iii P-value.
Abbreviations: BMI, body mass index; CI, confidence interval; DSM IV, Diagnostic and Statistical Manual for Mental Disorders, 4th edition; ePDs, edinburgh Postnatal Depression scale; Or, odds ratio; PPD, postpartum depression; sD, standard deviation.
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suhitharan et al
had their pregnancy planned, while 37% did not plan their pregnancy. Sixty-two (12.9%) patients were diagnosed with PPD. Univariate logistic regression analysis indicated that PPD was not significantly associated with females with high/ low economic status and high/basic education background, but was significantly associated with increasing age and number of children.
Table 2 shows 47 mothers (9.8%) had medical complica-tions during pregnancy. Among which, 33 females (6.9%) had gestational diabetes mellitus and 14 females (2.9%) had pregnancy-induced hypertension. However, there was no statistically significant difference between healthy mothers and mothers with medical complications in the outcome of PPD. Almost 10% of mothers with PPD had a medical condi-tion (diabetes mellitus, hypertension, and thyroid disease), whereas this number was much lower, 1.4%, in the group without PPD. A univariate analysis showed that females who had a history of peripartum depression or depression in the past were more likely to develop PPD. Sixteen out of 26 patients (61.5%) with a history of previous peripartum depression developed PPD, while only 46 out of 452 patients (10.2%) without past history of peripartum depression developed PPD during this study period. Similarly, six out of nine patients (66.7%) with past history of depression would develop PPD compared with 56 out of 469 (11.9%) patients without past history of depression would develop PPD.
The mode of delivery, whether it was vaginal delivery, instrumental delivery, or emergency Cesarean section, was not associated with increased risk of PPD (Table 3). Perinatal events such as maternal pyrexia and premature rupture of
membranes were not found to increase the risk of PPD. The duration of second stage of labor was significantly shorter in case group compared with control group. The numeric rating scale pain scores were similar between the PPD group and that of non-PPD group.
Table 4 shows epidural analgesia was performed in 329 females (68.7%). The unadjusted odds of PPD was sig-nificantly lower in females who received epidural analgesia (33 of 329 [10.0%]) than those who did not (29 of 150 [19.3%]) (P=0.0078). The use of Entonox was not associ-ated with decreased risk of PPD. The use of intramuscular pethidine on univariate analysis increased the risk of PPD. Nine of 32 females (28.1%) who had intramuscular pethidine developed PPD, whereas 52 of 445 females (11.7%) who did not receive intramuscular pethidine developed PPD.
Univariate logistic regression analysis showed that older age, multiple births, expected childcare by self/partner, any preexisting medical condition, any previous peripartum depression or any depression, any family history of depres-sion, use of epidural and pethidine during epidural analgesia increased the risk of PPD. These risk factors and other potential confounders (P#0.2) were considered for the multivariate logistic regression. Table 5 shows multivariate logistic regression analysis identified five independent risk factors for PPD. The absence of epidural analgesia was asso-ciated with higher risk of depression (adjusted OR 1.95, 95% CI 1.04–3.66, P=0.0367). Increasing age was associated with higher risk of PPD (adjusted OR 1.56, 95% CI 1.15–2.14,
P=0.005, for every 5 years increase). Other psychological factors associated with higher risk of PPD were family
Table 2 Maternal medical history
Characteristics Case (n=62), n (%) Control (n=417), n (%) Unadjusted OR (95% CI) P-value* Pregnancy complication: gestational diabetes
No 57 (93.44) 388 (93.05) reference
Yes 4 (6.56) 29 (6.95) 0.94 (0.32–2.77) 1.0000
Pregnancy complication: hypertension
No 57 (93.44) 407 (97.6) reference
Yes 4 (6.56) 10 (2.40) 2.86 (0.87–9.41) 0.0898
chronic medical conditions (diabetes mellitus, hypertension, thyroid)
No 55 (90.16) 410 (98.56) reference
Yes 6 (9.84) 6 (1.44) 7.45 (2.32–23.92) 0.0017
Family history of depression
No 48 (77.42) 406 (97.6) reference
Yes 14 (22.58) 10 (2.40) 11.84 (4.99–28.12) ,0.0001
history of depression
No 56 (90.32) 413 (99.28) reference
Yes 6 (9.68) 3 (0.72) 14.75 (3.59– 60.64) ,0.0001
Notes: Case represents patients with clinically confirmed diagnosis of PPD using DSM IV criteria of major depression of postpartum onset. control represents non-PPD patients with ePDs score #7. Unadjusted Ors were obtained from univariate logistic regression. *P-values were calculated based on Fisher’s exact test.
Abbreviations: CI, confidence interval; DSM IV, Diagnostic and Statistical Manual for Mental Disorders, 4th edition; ePDs, edinburgh Postnatal Depression scale; Or, odds ratio; PPD, postpartum depression.
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history of depression (adjusted OR 11.1, 95% CI 4.23–29.75,
P,0.0001), history of depression (adjusted OR 10.61, 95% CI 2.34–58.15, P=0.003), and previous history of PPD (adjusted OR 9.42, 95% CI 3.7–24.54, P,0.0001).
Discussion
Our study found that the odds of PPD were lower in females who received epidural analgesia for labor compared with those who chose nonepidural analgesia. We found a very strong association between development of PPD and previous history of depression or PPD and family history of depression.
Predisposing effect of these psychiatric risk factors has been well established and proved to be independent risk factors for PPD.10,19,20 Our finding of association between
increas-ing maternal age and higher risk of PPD (OR 1.56 for every 5-year increase) is similar to the finding of Canadian com-munity health survey, which identified the prevalence of depression in females who had recently delivered was sig-nificantly higher in females aged 40–44 years than in females aged 30–35 years (OR 3.72, 95% CI 2.15–6.41).21 This could
be due to the fact that older females have higher rates of multiple births and pregnancy complications, such as high
Table 3 Perinatal characteristics
Characteristics Case (n=62) Control (n=417) Unadjusted OR (95% CI) P-value Vaginal delivery, n (%)
No 13 (20.97) 84 (20.14) reference
Yes 49 (79.03) 333 (79.86) 1.05 (0.55–2.03) 0.8663*
instrumental delivery, n (%)
No 42 (87.50) 281 (84.13) reference
Yes 6 (12.50) 53 (15.87) 0.76 (0.31–1.87) 0.6717*
cesarean section, n (%)
No 50 (80.65) 336 (80.77) reference
Yes 12 (19.35) 80 (19.23) 0.99 (0.50–1.95) 1.0000*
Maternal pyrexia, n (%)
No 59 (95.16) 382 (91.61) reference
Yes 3 (4.84) 35 (8.39) 1.8 (0.54–6.05) 0.4533*
Premature rupture of membranes, n (%)
No 58 (93.55) 376 (90.17) reference
Yes 4 (6.45) 41 (9.83) 1.58 (0.55–4.58) 0.4904*
Duration of second stage labor (min)
Mean (sD) 28.96 (26.83) 54.85 (55.75) 0.98 (0.97–0.99) 0.0025#
Pain score recorded upon hospital admission
Mean (sD) 3.60 (3.91) 4.4 (3.81) 0.95 (0.88–1.02) 0.1256#
Pain score recorded during delivery
Mean (sD) 0.10 (0.65) 0.29 (1.37) 0.83 (0.58–1.18) 0.2977#
Notes: Case represents patients with clinically confirmed diagnosis of PPD using DSM IV criteria of major depression of postpartum onset. control represents non-PPD patients with ePDs score #7. Unadjusted Ors were obtained from univariate logistic regression. *P-values were calculated based on Fisher’s exact test. #P-values were
calculated based on student’s t-test.
Abbreviations: CI, confidence interval; DSM IV, Diagnostic and Statistical Manual for Mental Disorders, 4th edition; ePDs, edinburgh Postnatal Depression scale; Or, odds ratio; PPD, postpartum depression; sD, standard deviation.
Table 4 Primary outcome of PPD with regard to epidural analgesia and other modes of analgesia
Mode of analgesia Total (n=479) Case (n=62) Control (n=417) Unadjusted OR (95% CI) P-value epidural, n (%)
With 329 (68.7) 33 (53.23) 296 (70.98) 2.15 (1.25–3.7) 0.0078
Without 150 (31.3) 29 (46.77) 121 (29.02) reference
entonox, n (%)
With 203 (42.4) 29 (46.77) 174 (41.73) 1.23 (0.72–2.1) 0.4921
Without 276 (57.6) 33 (53.23) 243 (58.27) reference
Pethidine, n (%)
With 32 (8.5) 9 (14.52) 23 (5.53) 2.90 (1.28–6.6) 0.0242
Without 346 (91.5) 53 (85.48) 393 (94.47) reference
Notes: Case represents patients with clinically confirmed diagnosis of PPD using DSM IV criteria of major depression of postpartum onset. control represents non-PPD patients with ePDs score #7. Unadjusted Ors were obtained from univariate logistic regression. P-values were calculated based on Fisher’s exact test.
Abbreviations: CI, confidence interval; DSM IV, Diagnostic and Statistical Manual for Mental Disorders, 4th edition; ePDs, edinburgh Postnatal Depression scale; Or, odds ratio; PPD, postpartum depression.
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blood pressure and diabetes, which is associated with higher risk of PPD. We also proved the well-established independent psychiatric risk factors10,19 for the development of PPD, which
includes family history of depression, history of depression, and previous history of PPD. The independent association between absence of labor epidural analgesia and develop-ment of PPD was confirmed using multivariate regression analysis including other risk factors such as maternal age and the above-mentioned psychological factors.
The main strength of the study is use of clinical assess-ment, which is the gold standard for the diagnosis of PPD.6
This would explain the lower overall rate of PPD in our study population (12.9%) compared with the reported incidences of 24.3% from Asian study8 and 19.2% by a systematic review
on incidence and prevalence of PPD.22 Most of these studies
used EPDS to diagnose PPD. However, the researchers should note that the EPDS is not a diagnostic instrument, but rather a screening tool to detect depression in the postpartum period. Furthermore, a positive score could reflect a transient mood change rather than a depressive illness4 and eventually
overestimate the incidence of PPD. A cutoff score of 12 or 13 is typically used for “probable depression”, and as a marker for major depression, whereas a cutoff score of 9 or 10 is used for “possible” or minor depression.23
We found that the odds of PPD was lower in 10.0% (33/329) of females who received epidural analgesia com-pared with 19.3% (29/150) of those who choose nonepidural analgesia (OR 0.47 (0.27–0.8), P=0.0078). Furthermore, absence of epidural analgesia was identified as a factor that could almost double the risk of developing of PPD. Our finding is consistent with the observational study by Ding et al,8 in
which PPD occurred in 14.0% (15 of 107) of females who received epidural labor analgesia and in 34.6% (37 of 107) of those who did not have any analgesia (P,0.001). They also found epidural analgesia was associated with a decreased risk of PPD compared with having no analgesia at all
(OR 0.31, 95% CI 0.12–0.82, P=0.018).8 However, our study
methodology is different from Ding et al8 and Hiltunen et al.16
First, the diagnosis of PPD was made clinically by psychiatric specialist. Second, the above studies compared the effect of epidural analgesia on PPD with no analgesia at all. But we compared the epidural analgesia with nonepidural labor anal-gesic techniques such as Entonox or pethidine that replicates the real modern obstetric practice in many centers for labor analgesia, which is the strength of our study.
Limitations of our study are first due to the case–control design, where the exposure or outcome assessment maybe limited by recall bias of self-reported data during the psychi-atric assessment and effect of unknown confounding factors. Most of the data during the labor were obtained from maternal monitoring chart, case note documents, and epidural charts. This would minimize the effect of recall bias. The clinical diagnosis of PPD by a specialist psychiatrist than EPDS will further reduce the effect of recall bias on the outcome. We had to exclude nearly one-third of the medical records reviewed to ensure the data accuracy. However, we managed to analyze 479 patients who provided adequate information and analysis for this case–control design. Furthermore, we cannot determine the causal relationship of epidural analgesia on development of PPD with this study design. The majority of our study popula-tion are Singaporean Chinese females (98.5%) and no conclu-sions regarding females with different ethnic or socioeconomic groups may be drawn from this result. Lastly, we did not assess the psychological responses during labor that might be an important confounder. A woman who requested for epidural analgesia may have feelings of fear and insecurity, which might lead to increased risk of mood and depressive symptoms. The postpartum psychological assessment was done at 4–8 weeks with a median of 5 weeks postpartum and there is a possibility we could have missed detecting mild early PPD that resolved spontaneously during the psychological assessment.
Our study also showed other nonepidural labor analgesic techniques, like Entonox, mode of delivery, and pain scores after delivery, which were not associated with the develop-ment of PPD. The use of intramuscular pethidine may be associated with higher chance of development of PPD on the univariate analysis. This interesting finding corresponds to the published evidence from Robson and Kumar,24 who
found poor maternal affection toward the new born and Mohammad et al,25 who described a significant association
between development of PPD and pethidine use.
Conclusion
We conclude that use of labor epidural analgesia is associ-ated with a reduction of the odds of PPD compared with
Table 5 Multivariate logistics regression for risk factors for PPD
Risk factors Adjusted
OR (95% CI)
P-value
increase of maternal age* 1.56 (1.15–2.14) 0.0050
epidural (no vs yes) 1.95 (1.04–3.66) 0.0367
Family history of depression (yes vs no)
11.1 (4.23–29.75) ,0.0001
history of depression (yes vs no) 10.61 (2.34–58.15) 0.0031 Previous peripartum depression
(yes vs no)
9.42 (3.7–24.54) ,0.0001
Notes: adjusted Ors were obtained from multivariate logistic regression by taking potential confounders (P-value #0.2) identified by univariate analysis into the calculation. *every 5 year increase in age was associated with a higher risk of PPD. Abbreviations: CI, confidence interval; OR, odds ratio; PPD, postpartum depression.
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Mode of analgesia and risk of postpartum depression
nonepidural labor analgesic methods. Furthermore, absence of labor epidural analgesia is associated with the develop-ment of PPD. Prospective studies with larger sample size and a clinical confirmation of PPD is required to confirm the impact of epidural on PPD. These findings might help develop preventive strategies to decrease PPD through targeted evaluation and intervention. Further research is required to enable obstetricians and the anesthesiologists to have an evidence-based discussion with the pregnant females and the choice of epidural analgesia for labor pain.
Acknowledgments
We would like to acknowledge the administrative support from Ms Agnes Teo (Research Coordinator) and Ms Sarah Huan (Medical Student) and data collection by Jasmine Ng and Suzanne Tan (Research Assistants). We acknowl-edge the funding from the NMRC Clinical Trials Grant (CTG13feb013), NMRC Exploratory/Developmental Grant (NMRC/EDG/1006), and NMRC Centre Grant (NMRC/ CG/006/2013) in the conduct of research data collection and analysis for this manuscript.
Author contributions
All authors contributed toward data analysis, drafting, and revising the paper and agree to be accountable for all aspects of the work.
Disclosure
The authors report no conflicts of interest in this work.
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